Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

ADS Genes For Reducing Saturated Fatty Acid Levels In Seed Oils

a technology of saturated fatty acid and seed oil, which is applied in the field of lipid metabolism-related enzymes, can solve the problems that the fatty acid content alterations are not substantial enough to create truly meaningful new oilseeds, and achieve the effect of increasing saturated fatty acid

Active Publication Date: 2010-11-04
HEILMANN INGO H +1
View PDF33 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0013]In yet other embodiments, the present invention provides a method of decreasing saturated fatty acid in plant seed oil, comprising transforming a plant with a heterologous nucleic acid sequence comprising a first nucleic acid sequence operably linked to a seed specific promoter, wherein the first nucleic acid sequence comprises a nucleic acid which encodes an ADS polypeptide of SEQ ID NOs:2, 4, 6, or 8 or a protein that is at least 90% identical thereto and which has desaturase activity (e.g., SEQ ID NOs:1, 3, 5, and 7), and growing the plant under conditions such that the heterologous nucleic acid sequence is expressed and saturated fatty acid content in an oil of a seed of the plant is decreased.
[0014]In yet other embodiments, the present invention provides a method of decreasing palmitic acid and / or stearic acid in plant seed oil, comprising providing a plant comprising a heterologous nucleic acid sequence comprising a first nucleic acid sequence operably linked to a seed specific promoter, wherein the first nucleic acid sequence comprises a nucleic acid which encodes an ADS polypeptide of SEQ ID NOs:2, 4, 6, or 8 or a protein that is at least 90% identical thereto and which has desaturase activity (e.g., SEQ ID NOs:1, 3, 5, and 7), and growing the plant under conditions such that the nucleic acid sequence is expressed and palmitic acid and / or stearic acid in an oil of a seed of the plant is decreased.
[0015]In yet other embodiments, the present invention provides a method of increasing saturated fatty acid in plant seed oil, comprising providing a plant comprising a heterologous nucleic acid sequence comprising a first nucleic acid sequence operably linked to a seed specific promoter, wherein the first nucleic acid sequence comprises a nucleic acid which encodes an ADS polypeptide, an antisense sequence to a nucleic acid sequence which encodes SEQ ID NOs:2, 4, 6, or 8 or a protein that is at least 90% identical thereto and which has desaturase activity (e.g., an antisense sequence to SEQ ID NOs: 1, 3, 5, or 7), a sequence encoding an siRNA targeted to a sequence in a nucleic acid sequence which encodes an ADS polypeptide, a sequence encoding an siRNA targeted to a sequence in a nucleic acid sequence which encodes SEQ ID NOs:2, 4, 6, or 8 or a protein that is at least 90% identical thereto and which has desaturase activity (e.g., an siRNA targeted to a sequence in SEQ ID NOs: 1, 3, 5, or 7), and growing the plant under conditions such that the heterologous nucleic acid sequence is expressed and saturated fatty acid content of an oil of a seed of the plant is increased.
[0016]In yet other embodiments, the present invention provides a method of increasing saturated fatty acid in plant seed oil, comprising transforming a plant comprising a heterologous nucleic acid sequence comprising a first nucleic acid sequence operably linked to a seed specific promoter, wherein the first nucleic acid sequence comprises a nucleic acid which encodes an ADS polypeptide, an antisense sequence to a nucleic acid sequence which encodes SEQ ID NOs:2, 4, 6, or 8 or a protein that is at least 90% identical thereto and which has desaturase activity (e.g., an antisense sequence to SEQ ID NOs: 1, 3, 5, or 7), a sequence encoding an siRNA targeted to a sequence in a nucleic acid sequence which encodes an ADS polypeptide, a sequence encoding an siRNA targeted to a sequence in to a nucleic acid sequence which encodes SEQ ID NOs:2, 4, 6, or 8 or a protein that is at least 90% identical thereto and which has desaturase activity (e.g., a sequence encoding an siRNA targeted to a sequence in SEQ ID NOs: 1, 3, 5, or 7), and growing the plant under conditions such that the heterologous nucleic acid sequence is expressed and saturated fatty acid content of an oil of a seed of the plant is increased.
[0017]In yet other embodiments, the present invention provides a method of increasing unsaturated acid in plant seed oil, comprising providing a plant comprising a heterologous nucleic acid sequence comprising a first nucleic acid sequence operably linked to a seed specific promoter, wherein the first nucleic acid sequence comprises a nucleic acid sequence which encodes an ADS polypeptide, a nucleic acid sequence which encodes SEQ ID NOs:2, 4, 6, or 8 or a protein that is at least 90% identical thereto and which has desaturase activity (e.g., SEQ ID NOs:1, 3, 5, and 7), and growing the plant under conditions such that the heterologous nucleic acid sequence is expressed and unsaturated fatty acid in an oil of a seed of the plant is decreased.
[0018]In yet other embodiments, the present invention provides a method of increasing palmitoleic acid and / or vaccenic acid in plant seed oil, comprising providing a plant comprising a heterologous nucleic acid sequence comprising a first nucleic acid sequence operably linked to a seed specific promoter, wherein the first nucleic acid sequence comprises a nucleic acid sequence which encodes an ADS polypeptide, a nucleic acid sequence which encodes SEQ ID NOs:2, 4, 6, or 8 or a protein that is at least 90% identical thereto and which has desaturase activity (e.g., SEQ ID NOs:1, 3, 5, and 7), and growing the plant under conditions such that the heterologous nucleic acid sequence is expressed and palmitoleic acid and / or vaccenic acid in an oil of a seed of the plant is decreased.

Problems solved by technology

However, to date, the alterations in fatty acid content have not been substantial enough to create truly meaningful new oilseed lines.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • ADS Genes For Reducing Saturated Fatty Acid Levels In Seed Oils
  • ADS Genes For Reducing Saturated Fatty Acid Levels In Seed Oils
  • ADS Genes For Reducing Saturated Fatty Acid Levels In Seed Oils

Examples

Experimental program
Comparison scheme
Effect test

example 1

Materials and Methods

[0300]This example describes the materials and methods used in the characterization of ADS genes.

Yeast Growth and Transformation

[0301]The DTY10A-derived yeast strain DTY11A disrupted in the OLE1 gene and exhibiting no endogenous fatty acid desaturation was used as a host for complementation experiments. Cultures were initiated from single colonies and grown at 30° C. in synthetic complete medium without uracil, pH 6, containing 4% (w / w) glycerol and 0.8% (w / w) glucose (SC-ura). For growth of DTY11A, SC-ura was supplemented with 5 mM each of palmitoleic and oleic acid in final 0.1% (w / w) tergitol (SC-ura+FA). Solid media contained 1.2% (w / w) agar, 18% (w / w) sorbitol, and 1% (w / w) tergitol.

[0302]For growth experiments, 5-ml DTY11A cultures were grown in SC-ura+FA over night at 30° C. shaking at 150 rpm up to an optical density (OD) of approximately 2. Cells were pelleted by centrifugation, washed once in SC-ura and carefully resuspended. With the obtained cell mat...

example 2

Characterization of ADS Genes

[0313]This example describes the results of experiments characterizing ADS genes.

Expression of ADS1, ADS2 and ADS372-371 in the Yeast Unsaturated Fatty Acid Auxotroph DTY11A Overcomes the Requirement for Unsaturated Fatty Acid Supplementation.

[0314]In order to functionally test the ADS desaturases, whether they would complement an unsaturated fatty acid auxotroph DTY11A, a yeast strain in which the Δ9-stearoyl-CoA desaturase had been deleted, was examined. ADS1, ADS2 and ADS3 minus its transit peptide (ADS372-371) were expressed under the GAL1 promoter. Functional complementation was observed with all three constructs, because significant growth was observed in the absence of desaturated fatty acid supplementation (FIG. 2). The growth rates observed were slower that those for parental lines containing the endogenous yeast desaturase. Rates were somewhat variable between experiments, and complementation was not observed on solid media. Expression of Yep35...

example 3

Switching of Desaturase Specificity

A. Materials and Methods

[0319]cDNA Constructs

[0320]For yeast expression, cDNAs for ADS1, ADS2 and ADS3 lacking a transit peptide coding sequence (i.e. ADS372-371) were generated by polymerase chain reaction (PCR) from Arabidopsis flower cDNA using the primer combinations 5′-GCCTGGATCCATGTCATTGTCAGCCTCGGAGAAGG-3′ (SEQ ID NO:30) / 5′-CAGTGAGCTCCGAGACGTCGTTCCATATCTTCAACG-3′ (SEQ ID NO:31), 5′-GCCTGGATCCATGTCGGTGACATCAACGGTGG-3′ (SEQ ID NO:32) / 5′-CAGTGAGCTCTCAACGAACTATAGCCATACGACG-3′ (SEQ ID NO:33), and 5′-GCATGGATCCATGGGAGATTACAGAAGGATA-3′ (SEQ ID NO:34) / 5′-CAGTGAATTCATACCTTTAAGTAAACACAAAAAAGC-3′ (Primer A; SEQ ID NO:35), respectively. The complete ADS3 coding region was amplified using the primer combination 5′-CAGTGGATCCTAAGTTAAGGGTTTAAGCCTCTTCTC-3′ (SEQ ID NO:36) / Primer A. ADS1, ADS2, and ADS372-371 were inserted as BamHI / SacI fragments into Yep352YOPR (Shanklin et al., (1994) Biochemistry 33, 12787-12794) and as BamHI / EcoRI fragments into the yeast ...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
nucleic acid sequenceaaaaaaaaaa
concentrationaaaaaaaaaa
structuresaaaaaaaaaa
Login to View More

Abstract

The present invention relates to enzymes involved in lipid metabolism. In particular, the present invention provides coding sequences for Arabidopsis Desaturases (ADS), the encoded ADS polypeptides, and methods for using the sequences and encoded polypeptides, where such methods include decreasing and increasing saturated fatty acid content in plant seed oils.

Description

[0001]This Application claims priority to provisional patent application Ser. No. 60 / 474,045, filed May 29, 2003, which is herein incorporated by reference in its entirety.[0002]The present application was funded in part with government support under grant number DE-AC02-98CH10886, awarded by the US Department of Energy. The government may have certain rights in this invention.FIELD OF THE INVENTION[0003]The present invention relates to enzymes involved in lipid metabolism. In particular, the present invention provides coding sequences for Arabidopsis Desaturase (ADS), the encoded ADS polypeptides, and methods for using the sequences and encoded polypeptides, where such methods include decreasing and increasing saturated fatty acid content in plant seed oils.BACKGROUND OF THE INVENTION[0004]Plant metabolism has evolved the ability to produce a diverse range of structures, including more than 20,000 different terpenoids, flavonoids, alkaloids, and fatty acids. Fatty acids have been e...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(United States)
IPC IPC(8): C12N15/82C07H21/04C12N9/02
CPCC07H21/04C12N15/8247C12N9/0083
Inventor HEILMANN, INGO H.SHANKLIN, JOHN
Owner HEILMANN INGO H
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com